Kyowa Kirin
The Associate Director, Quality Control will lead the design and execution of the operational readiness program for start‑up of QC laboratories at Kyowa Kirin's new monoclonal antibody drug substance manufacturing facility in Sanford, NC. This role will manage greenfield lab start‑up, transition to GMP‑ready operations, and ensure compliance with GxP standards while overseeing staff, method implementation, and regulatory readiness.
Kyowa Kirin is a Japanese biopharmaceutical company that develops innovative specialty medicines, with a particular focus on antibody‑based therapies for cancer, kidney disease, and immune‑mediated disorders. The company pursues technology‑driven drug discovery across biologics and small molecules and maintains a broad global network of research, development, and commercial operations. Kyowa Kirin advances a pipeline through internal R&D and strategic partnerships (including biologics and CDMO collaborations) to bring life‑changing treatments to patients. It emphasizes patient‑centred value, scientific expertise, and sustainability in its mission to raise health and well‑being worldwide.
Kyowa Kirin Integrates North America Businesses in Support of Company's 2030 Vision and Rapid Growth Trajectory
Mar 31, 2021
La Jolla Institute renews longtime collaboration with Kyowa Kirin, Inc.
Jan 18, 2022
Kyowa Kirin Completes New North American Headquarters in Princeton
Jul 11, 2023
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Kyowa Kirin.
6% below the average for this role
How Kyowa Kirin is Giving Employees a Voice in the Company’s Future
Dec 7, 2023
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